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COCOMUSE, HPM38 (polymacon) Daily Wear Soft (hydrophilic) Contact Lens

by Hunan Haipuming Technology Co., Ltd. 444 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06942686571495 UDI-DI Date13 Jul 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Soft corrective contact lens, daily-disposable
Model / Reference
HPM38
Primary DI / UDI-DI
06942686571495
510(k) Number
FDA Product Code
LPL, MVN
GMDN Term
Soft corrective contact lens, daily-disposable
Device Class
Class II
Regulation Number
886.5925
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K241884)

Show all (12)

Other devices from Hunan Haipuming Technology Co., Ltd.

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Properties

  • Sterile
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No